Ad-Tech Medical Instrument Corporation - FDA 510(k) Cleared Devices
Recent clearances: Spencer Probe Depth Electrodes, Anchor Bolts as Accessories to Depth Electrodes, Subdural Strip/Intraoperative Split Electrode, Subdural Grid/Intraoperative Grid Electrode, Dual-Sided Interhemispheric Subdural Electrode, Multi-Strip and Slit Grid Subdural Electrode, Intraoperative Mapping Grid Subdural Electrode
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ad-Tech Medical Instrument Corporation Ear, Nose, Throat ✕
1 devices